Clinical Trial Management Intern

We are seeking a motivated and detail-oriented **Clinical Trial Management Intern** to join our dynamic team. This role is an exciting opportunity to immerse yourself in the world of clinical research, supporting the execution of late-phase clinical trials. You’ll work alongside experienced professionals, gaining invaluable insights into clinical trial operations while contributing to impactful projects that drive innovation in healthcare. As a valued team member, you’ll collaborate with clinical study teams, ensure compliance with regulatory standards, and play a vital role in maintaining operational excellence. If you’re passionate about clinical research and eager to learn, this internship offers an incredible platform to grow and make a difference. A Typical Day: In this role, you’ll engage in diverse responsibilities that provide a comprehensive view of clinical trial management. Your day may include: * Coordinating and attending Clinical Study Team (CST) meetings, preparing agendas, materials, and minutes. * Supporting the organization of events such as investigator meetings and team sessions. * Tracking site study start-up activities and maintaining study tools for progress monitoring. * Assisting in the collection, review, and quality control (QC) of essential study documents and the electronic Trial Master File (eTMF). * Collaborating with the eTMF lead to ensure study documentation is accurate, complete, and timely. * Compiling and assembling study binders, reference manuals, and training materials under the guidance of clinical study leaders. * Managing and updating team SharePoint or shared drive sites as needed. * Participating in other CTM projects as assigned by the Senior Director of Clinical Trial Management. This Role May Be For You If: You’re a proactive and organized individual who thrives in a collaborative environment. You may excel in this role if: * You enjoy working with global teams and communicating with diverse stakeholders. * You’re detail-oriented and capable of juggling multiple tasks while maintaining accuracy. * You’re comfortable using Microsoft Word, Excel, Outlook, and PowerPoint. * You’re eager to learn and contribute to a fast-paced clinical research environment. * You’re confident in your ability to support administrative and operational aspects of clinical trials. * You’re motivated to maintain high-quality standards in compliance with FDA regulations, GCP, and ICH guidelines. To Be Considered: To qualify for this internship, you must: * Be enrolled full-time in a Bachelor’s, Master’s, or PhD program at an accredited university. * Be continuing your studies full-time after completing the internship at Regeneron Pharmaceuticals Inc. * Demonstrate excellent interpersonal, collaboration, and communication skills. * Show a proactive, self-motivated, and organized approach to work. This is your chance to contribute to meaningful clinical research while building a foundation for your future career. Join us at Regeneron Pharmaceuticals Inc., where innovation meets opportunity. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.